Wockhardt gets USFDA nod for Ranitidine syrup

Source: IRIS (24 February 2009)

Wockhardt gets USFDA nod for Ranitidine syrup
Email      Print   

Wockhardt has received final approval from the US Food and Drug Administration (USFDA) to market Ranitidine syrup, in the strength of 15 mg.

Ranitidine is used in treatment of peptic ulcer disease (PUD) and gastroesophageal reflux disease (GERD). It is also used alongside fexofenadine and other antihistamines for the treatment of skin conditions such as hives.

Recently, the company had received final approval from the US Food and Drug Administration (USFDA) to market Sumatriptan Succinate injectable/ injection, in the strength of 6 mg and 0.5 ml.

Shares of the company closed down Rs 3, or 3.29%, at Rs 88.30. The total volume of shares traded was 20,781 at the BSE (Friday).



* Q - Quote , N - News , C - Chart , F - Financials


  Print this article   Email to friend    Rate this article
 

 

Home | Shares | F&O | Mutual Funds | Loans | Credit cards | News Centre
Trade On-line | Wealth Tracker | Myiris radio | Newsletters | Tax Corner | NRI Centre | Forums | E-mail | Chat | Search in myiris
© A All rights reserved. IRIS Business Services Private Limited
Disclaimer